A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106077



Internal ID21506435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53921419..53921659hg38UCSC Ensembl
chr19:54424673..54424913hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599168
Supporting Variants
SamplesNA19983
Known GenesCACNG7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106077
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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